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A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies.

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Title: A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies.
Authors: Pode-Shakked, Ben1,2,3,4 (AUTHOR) Ben.PodeShakhed@sheba.health.gov.il, Barel, Ortal5,6 (AUTHOR), Singer, Amihood7 (AUTHOR), Regev, Miriam1,4 (AUTHOR), Poran, Hana1,4 (AUTHOR), Eliyahu, Aviva1,4 (AUTHOR), Finezilber, Yael1,4,8 (AUTHOR), Segev, Meirav1,4 (AUTHOR), Berkenstadt, Michal1,4 (AUTHOR), Yonath, Hagith1,4,8 (AUTHOR), Reznik-Wolf, Haike1,4 (AUTHOR), Gazit, Yael1,4 (AUTHOR), Chorin, Odelia1,2,4 (AUTHOR), Heimer, Gali3,4,9 (AUTHOR), Gabis, Lidia V.4 (AUTHOR), Tzadok, Michal4,9 (AUTHOR), Nissenkorn, Andreea4,9,10 (AUTHOR), Bar-Yosef, Omer3,4,9 (AUTHOR), Zohar-Dayan, Efrat4,9 (AUTHOR), Ben-Zeev, Bruria4,9 (AUTHOR)
Source: Scientific Reports. 9/27/2021, Vol. 11 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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Description
ISSN:20452322
DOI:10.1038/s41598-021-98646-w